A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067067



Internal ID19156286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32069540..32904180hg38UCSC Ensembl
Innerchr16:32080861..32915501hg19UCSC Ensembl
Innerchr16:31988362..32823002hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38834641
hg19834641
hg18834641
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2841n100
Supporting Variantsnssv3549342, nssv3549341
Samples
Known GenesHERC2P4, LOC390705, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067067
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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